State Key Laboratory of Oral Disease & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, People's Republic of China.
Department of Pediatric Dentistry, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, People's Republic of China.
Biomed Mater. 2024 May 17;19(4). doi: 10.1088/1748-605X/ad475c.
Hard tissue engineering scaffolds especially 3D printed scaffolds were considered an excellent strategy for craniomaxillofacial hard tissue regeneration, involving crania and facial bones and teeth. Porcine treated dentin matrix (pTDM) as xenogeneic extracellular matrix has the potential to promote the stem cell differentiation and mineralization as it contains plenty of bioactive factors similar with human-derived dentin tissue. However, its application might be impeded by the foreign body response induced by the damage-associated molecular patterns of pTDM, which would cause strong inflammation and hinder the regeneration. Ceria nanoparticles (CNPs) show a great promise at protecting tissue from oxidative stress and influence the macrophages polarization. Using 3D-bioprinting technology, we fabricated a xenogeneic hard tissue scaffold based on pTDM xenogeneic TDM-polycaprolactone (xTDM/PCL) and we modified the scaffolds by CNPs (xTDM/PCL/CNPs). Through series ofverification, we found xTDM/PCL/CNPs scaffolds held promise at up-regulating the expression of osteogenesis and odontogenesis related genes including collagen type 1, Runt-related transcription factor 2 (RUNX2), bone morphogenetic protein-2, osteoprotegerin, alkaline phosphatase (ALP) and DMP1 and inducing macrophages to polarize to M2 phenotype. Regeneration of bone tissues was further evaluated in rats by conducting the models of mandibular and skull bone defects. Theevaluation showed that xTDM/PCL/CNPs scaffolds could promote the bone tissue regeneration by up-regulating the expression of osteogenic genes involving ALP, RUNX2 and bone sialoprotein 2 and macrophage polarization into M2. Regeneration of teeth evaluated on beagles demonstrated that xTDM/PCL/CNPs scaffolds expedited the calcification inside the scaffolds and helped form periodontal ligament-like tissues surrounding the scaffolds.
硬组织工程支架,特别是 3D 打印支架,被认为是颅颌面硬组织再生的一种极好策略,涉及颅骨、面骨和牙齿。猪处理牙本质基质(pTDM)作为异种细胞外基质,具有促进干细胞分化和矿化的潜力,因为它含有大量与人类牙本质组织相似的生物活性因子。然而,其应用可能会受到 pTDM 损伤相关分子模式引起的异物反应的阻碍,这会导致强烈的炎症并阻碍再生。氧化铈纳米粒子(CNPs)在保护组织免受氧化应激方面显示出巨大的潜力,并影响巨噬细胞的极化。我们使用 3D 生物打印技术,制造了一种基于 pTDM 异种 TDM-聚己内酯(xTDM/PCL)的异种硬组织支架,并通过 CNPs 对支架进行了修饰(xTDM/PCL/CNPs)。通过一系列验证,我们发现 xTDM/PCL/CNPs 支架有望上调骨生成和牙发生相关基因的表达,包括胶原蛋白 1、Runt 相关转录因子 2(RUNX2)、骨形态发生蛋白 2、骨保护素、碱性磷酸酶(ALP)和 DMP1,并诱导巨噬细胞向 M2 表型极化。通过进行下颌骨和颅骨缺损模型,在大鼠中进一步评估了骨组织的再生。评估结果表明,xTDM/PCL/CNPs 支架通过上调涉及 ALP、RUNX2 和骨唾液蛋白 2 的成骨基因的表达以及巨噬细胞向 M2 的极化来促进骨组织的再生。在比格犬上进行的牙齿再生评估表明,xTDM/PCL/CNPs 支架加速了支架内的钙化,并有助于形成围绕支架的牙周韧带样组织。